Senior Statistical Programmer FSP

Cytel (EMEA); Remote; GBP 60,000 - 80,000; Full time

Job summary

A pharmaceutical consulting firm is looking for a Senior Statistical Programmer to support Phase I-IV clinical trials. The role demands advanced SAS programming skills and expertise in CDISC standards. Responsibilities include analyzing clinical trial data, generating datasets, and creating detailed reports. Ideal candidates should have at least 8 years of experience in the Pharma/Biotech sector, strong analytical capabilities, and the ability to thrive in a dynamic team environment. This position offers the flexibility of remote work.

Benefits

Collaborative work environment

Autonomy in role

Support of a dedicated client team

Qualifications

• 8+ years of SAS programming experience in clinical trials within Pharma/Biotech.
• Experience implementing CDISC SDTM/ADaM standards.
• Ability to manage multiple studies simultaneously.

Responsibilities

• Perform data manipulation, analysis, and reporting of clinical trial data.
• Generate and validate SDTM and ADaM datasets.
• Create and QC submission documents.

Skills

SAS programming

CDISC standards

Data manipulation and reporting

Efficacy analysis

Validation skills

Ad-hoc reporting

Analytical skills

Education

Bachelor's degree in Statistics, Computer Science, Mathematics

Job description

As a Senior Statistical Programmer, you will leverage your advanced SAS programming skills and proficiency in CDISC standards (SDTM & ADaM) to support or lead one or more Phase I-IV clinical trials. This role can be performed as fully remote.

Responsibilities

• Performing data manipulation, analysis and reporting of clinical trial data, both safety and efficacy (ISS/ISE), utilizing SAS programming
• Generating and validating SDTM and ADaM datasets/analysis files, and tables, listings, and figures (TLFs)
• Production and QC / validation programming
• Generating complex ad-hoc reports utilizing raw data
• Applying strong understanding/experience of Efficacy analysis
• Creating and reviewing submission documents and eCRTs
• Communicating with and/or responding to internal cross-functional teams and client for project specifications, status, issues or inquiries
• Performing lead duties when called upon
• Serving as team player, with a willingness to go the extra distance to get results, meet deadlines, etc.
• Being adaptable and flexible when priorities change

Qualifications

• Bachelor's degree in one of the following fields Statistics, Computer Science, Mathematics, etc.
• At least 8 years of SAS programming working with clinical trial data in the Pharmaceutical & Biotech industry with a bachelor's degree or equivalent. At least 6 years of related experience with a master's degree or above.
• Study lead experience, preferably juggling multiple projects simultaneously preferred.
• Strong SAS data manipulation, analysis and reporting skills.
• Solid experience implementing the latest CDISC SDTM / ADaM standards.
• Strong QC / validation skills.
• Good ad-hoc reporting skills.
• Proficiency in Efficacy analysis.
• Familiarity with drug development life cycle and experience with the manipulation, analysis and reporting of clinical trials' data.
• Submissions experience utilizing define.xml and other submission documents.
• Experience supporting immunology, respiratory or oncology studies would be a plus.
• Excellent analytical & troubleshooting skills.
• Ability to provide quality output and deliverables, in adherence with challenging timelines.
• Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners.

Benefits & Company

• Working fully embedded within one of our pharmaceutical clients, with the support of Cytel right behind you, you'll be at the heart of our client's innovation. As a Senior Statistical Programmer you will be dedicated to one of our global pharmaceutical clients; a company that is driving the next generation of patient treatment, where individuals are empowered to work with autonomy and ownership. This is an exciting time to be a part of this new program.
• We nurture intellectual curiosity and encourage everyone to approach new challenges with enthusiasm and the desire for discovery.
• We believe in collaboration and invite a diversity of perspectives, drawing on a variety of talents to create a wealth of possibilities.
• We prize innovation and seek intelligent solutions using leading-edge technology.